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<br />. <br />. <br /> <br />VOL. 102, NO, 3, JULY 1983 <br /> <br />247 <br /> <br />(1980) made no mention of their distribution on E. salvelini, Tedesco & Cog- <br />gins (1980) speculated that tumuli may serve in eccrine secretion. However, <br />the functional significance of tumuli has not been elucidated, so it is difficult <br />to explain the distribution of these structures along the strobila. <br />The outer portion of the tegument of B. acheilognathi was composed of a <br />dense layer of microtriches, and while their morphology is somewhat differ- <br />ent between the scolex and the proglottids, each area possesses microtriches <br />of a single form. Scolex microtriches are longer and thinner than those on the <br />strobila. This apparent dimorphism, however, is not consistent for all cestode <br />species. For example, Thompson et aI. (1980) observed morphologic and size <br />differences among microtriches on the strobila and scolex, as well as differ- <br />ences within the same region of Proteocephalus tidswelli, Several investi- <br />gators have reported on the distribution of two types of microtriches found <br />on Mesocestoides corti (Hess, 1981; Hess & Guggenheim, 1977; Voge et aI., <br />1979). Both filamentous and blade-like microtriches occur behind the suckers; <br />only filamentous forms are found at the posterior end of the strobila. Berger <br />& Mettrick (1971) reported that Hymenolepis diminuta has two morpholog- <br />ically distinct types of microtriches on the mature and gravid segments. Sim- <br />ilar patterns of microthrix distribution occur on H. nana and H, microstoma, <br />although the direction in which these structures bend varies among the three <br />species. <br />Microtriches within the bothria of B. acheilognathi are somewhat more <br />slender in appearance than microtriches on the adjacent outer tegument. An- <br />dersen (1975) also noted a similar appearance of the microtriches within the <br />bothria of Diphyllobothrium dendriticum, D. ditremum, and D, latum, but <br />the functional significance of these slender structures is not known, <br />Sensory cilia (sensilla) are spaced between microtriches of the strobila. <br />These structures were observed only in the tegument of proglottids and were <br />not seen within the scolex tegument. This observation is in contrast to that <br />of Jones (1975), who found sensory cilia in the tegument of the scolex of <br />Bothriocephalus scorpii but not on the strobila. <br />Webb & Davey (1974) conducted a thorough ultrastructural study of sensory <br />receptors in a cestode species. These investigators described two different <br />types of sensory structures from Hymenolepis microstoma. The sensory cilia <br />found in the tegument of the strobila of B. acheilognathi most closely resem- <br />ble the sensilla described from the scolex of H. microstoma, Both are char- <br />acte),"ized by a rather long cilium and the absence of ciliary rootlets. There <br />are two electron-dense collars within the dendritic bulb of the sensilla of H. <br />microstoma, but only one such collar is present in the bulb of B, acheilo- <br />gnathi. Moreover, sensilla of B, acheilognathi possess microtubules and a <br />few electron-lucent vesicles, Sensory bulbs of H. microstoma are packed with <br />such vesicles; microtubules were not discernible. The dendritic bulb of Rail- <br />lietina cesticillus possesses both electron-lucent vesicles and microtubules <br />(Blitz & Smyth, 1973), <br />Electron-dense collars appear to be a common feature of the sensilla of <br />